Canonical Allele Identifier: CA1619116508

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354139_31354140delinsAG , CM000668.2:g.31354139_31354140delinsAG	GRCh38
NC_000006.11:g.31321916_31321917delinsAG , CM000668.1:g.31321916_31321917delinsAG	GRCh37
NC_000006.10:g.31429895_31429896delinsAG	NCBI36
NG_023187.1:g.8073_8074delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3297_3298delinsCT
ENST00000481849.6:n.3257_3258delinsCT
ENST00000497377.6:n.3164_3165delinsCT
ENST00000696558.1:c.1319_1320delinsCT	ENSP00000512716.1:n.1319_1320delinsCT
ENST00000696559.1:c.*161_*162delinsCT	ENSP00000512717.1:n.*161_*162delinsCT
ENST00000696560.1:c.*161_*162delinsCT	ENSP00000512718.1:n.*161_*162delinsCT
ENST00000696561.1:c.*161_*162delinsCT	ENSP00000512719.1:n.*161_*162delinsCT
ENST00000696562.1:c.*161_*162delinsCT	ENSP00000512720.1:n.*161_*162delinsCT
ENST00000412585.7:c.*161_*162delinsCT MANE Select	ENSP00000399168.2:n.*161_*162delinsCT
ENST00000412585.6:c.*161_*162delinsCT	ENSP00000399168.2:n.*161_*162delinsCT
ENST00000481849.5:n.485_486delinsCT
ENST00000497377.5:n.649_650delinsCT
NM_005514.6:c.*161_*162delinsCT	NP_005505.2:n.*161_*162delinsCT
XM_011514556.1:c.*161_*162delinsCT	XP_011512858.1:n.*161_*162delinsCT
XM_011514557.1:c.*161_*162delinsCT	XP_011512859.1:n.*161_*162delinsCT
XR_926175.1:n.1689_1690delinsCT
NM_005514.7:c.*161_*162delinsCT	NP_005505.2:n.*161_*162delinsCT
NM_005514.8:c.*161_*162delinsCT MANE Select	NP_005505.2:n.*161_*162delinsCT